Our Vision: A quality of life for people living with MND which is not compromised by their diagnosis - a life with dignity and independence.


The MND and Me Foundation Limited is a not for profit organisation that was formed to raise awareness of Motor Neurone Disease (MND) and its' impact in the community. We saw the desperate need to assist people living with MND and their families to maintain their independence and quality of life for as long as possible. The Foundation intends to contribute financially toward research into finding a cure, but until one is found, our major objectives are to ensure those who have to live with this terrible disease and their families are supported by the Foundation both in financial and non-financial ways.


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Latest News & Events

SULLY’S EULOGY – THE LIFE OF A GREAT MAN

Protected: SULLY’S EULOGY – THE LIFE OF A GREAT MAN

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We understand numerous people outside the church on the d…
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Million Metres for MND Team at GC Marathon – JOIN NOW !!

Million Metres for MND Team at GC Marathon – JOIN NOW !!

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2014 Million Metres for MND team…
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THE LONG GOODBYE

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THE LONG GOODBYE

Enter the world of Scott Sullivan, an ordinary man showing extra…
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Muscle Up MND 2014

http://youtu.be/FeEAJuB7Gqw

1810 “Muscle Uppers” attempting to break the world record for the largest personal t…
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2014 Muscle up for MND

http://youtu.be/xfmVZU3BE5E

2014 Muscle up for MND…
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2013 MND and Me Foundation Year in Review

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2013 MND and Me Foundation Year in Review

A big thank you to all our amazing supp…
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Who is Scott Sullivan?

2013 MND and Me Foundation Year in Review


Awarded 2011 Queensland ‘Pride of Australia Medal’ for Courage

Scott Sullivan is a 39 year old vibrant, fun-loving and energetic husband and father of two young children. On October 22, 2010 he was diagnosed with Motor Neurone Disease (MND) – a disease with no known cause, no known cure and no effective treatment. His life expectancy is 3-5 years.

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